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dr. M.S. (Matthijs) Berends
2026-06-23 01:20:09 +02:00
parent 57e45db320
commit f0c3ce80cd
14 changed files with 95 additions and 82 deletions
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2
man/g.test.Rd
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@@ -46,7 +46,7 @@ A list with class \code{"htest"} containing the following
\code{(observed - expected) / sqrt(expected)}.}
\item{stdres}{standardized residuals,
\code{(observed - expected) / sqrt(V)}, where \code{V} is the
residual cell variance (Agresti, 2007, section 2.4.5
residual cell variance {(\if{html}{\out{<a href="#reference+chisq.test.Rd+R+3AAgresti+3A2007" class="citation">}}Agresti 2007\if{html}{\out{</a>}}, section 2.4.5)}
for the case where \code{x} is a matrix, \code{n * p * (1 - p)} otherwise).}
}
\description{

5
man/ggplot_pca.Rd
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@@ -42,8 +42,9 @@ ggplot_pca(x, choices = 1:2, scale = 1, pc.biplot = TRUE,
}
\item{pc.biplot}{
If true, use what Gabriel (1971) refers to as a "principal component
biplot", with \code{lambda = 1} and observations scaled up by sqrt(n) and
If true, use what {\if{html}{\cite{}\out{<a href="#reference+biplot.princomp.Rd+R+3AGabriel+3A1971" class="citation">}}Gabriel (1971)\if{html}{\out{</a>}}} refers to as a
\dQuote{principal component biplot},
with \code{lambda = 1} and observations scaled up by sqrt(n) and
variables scaled down by sqrt(n). Then inner products between
variables approximate covariances and distances between observations
approximate Mahalanobis distance.

2
man/mo_property.Rd
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@@ -200,7 +200,7 @@ All functions will, at default, \strong{not} keep old taxonomic properties, as s
The short name (\code{\link[=mo_shortname]{mo_shortname()}}) returns the first character of the genus and the full species, such as \code{"E. coli"}, for species and subspecies. Exceptions are abbreviations of staphylococci (such as \emph{"CoNS"}, Coagulase-Negative Staphylococci) and beta-haemolytic streptococci (such as \emph{"GBS"}, Group B Streptococci). Please bear in mind that e.g. \emph{E. coli} could mean \emph{Escherichia coli} (kingdom of Bacteria) as well as \emph{Entamoeba coli} (kingdom of Protozoa). Returning to the full name will be done using \code{\link[=as.mo]{as.mo()}} internally, giving priority to bacteria and human pathogens, i.e. \code{"E. coli"} will always be considered \emph{Escherichia coli}. As a result, \code{mo_fullname(mo_shortname("Entamoeba coli"))} returns \code{"Escherichia coli"}.
Following the formal introduction of the new kingdom rank into prokaryotic nomenclature by G\u00f6ker and Oren (2024, \doi{10.1099/ijsem.0.006242}), \code{\link[=mo_kingdom]{mo_kingdom()}} and \code{\link[=mo_domain]{mo_domain()}} return different results for bacteria and archaea: \code{\link[=mo_kingdom]{mo_kingdom()}} returns the new formal kingdom (e.g. "Pseudomonadati", "Bacillati"), while \code{\link[=mo_domain]{mo_domain()}} returns the new domain (e.g. "Bacteria", "Archaea"). For non-prokaryotic organisms, both functions return identical results.
Following the formal introduction of the new kingdom rank into prokaryotic nomenclature by G"{o}ker and Oren (2024, \doi{10.1099/ijsem.0.006242}), \code{\link[=mo_kingdom]{mo_kingdom()}} and \code{\link[=mo_domain]{mo_domain()}} return different results for bacteria and archaea: \code{\link[=mo_kingdom]{mo_kingdom()}} returns the new formal kingdom (e.g. "Pseudomonadati", "Bacillati"), while \code{\link[=mo_domain]{mo_domain()}} returns the new domain (e.g. "Bacteria", "Archaea"). For non-prokaryotic organisms, both functions return identical results.
Determination of human pathogenicity (\code{\link[=mo_pathogenicity]{mo_pathogenicity()}}) is strongly based on Bartlett \emph{et al.} (2022, \doi{10.1099/mic.0.001269}). This function returns a \link{factor} with the levels \emph{Pathogenic}, \emph{Potentially pathogenic}, \emph{Non-pathogenic}, and \emph{Unknown}.